510(k) K202393

Device
SpineJack Expansion Kit
Applicant
Stryker Corporation
510(k) number
K202393
Product code
NDN
Decision
Substantially Equivalent (SESE)
Decision date
2020-10-20
Date received
2020-08-21
Regulation
888.3027
Classification name
Cement, Bone, Vertebroplasty
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Kristi Ashton
Address
1926 Stryker Way Portage MI US 49002 49002

FDA Registration Numbers

Source Documents

510(k) summary PDF

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